Variant report

Variant	esv2752073
Chromosome Location	chr5:60034475-60136626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:610)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
2	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
3	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
4	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
5	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
6	ATF2	chr5:60122399-60122938	GM12878	blood:	n/a	n/a
7	ATF2	chr5:60122280-60122899	GM12878	blood:	n/a	n/a
8	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
9	BATF	chr5:60117975-60118244	GM12878	blood:	n/a	n/a
10	BATF	chr5:60034409-60034644	GM12878	blood:	n/a	n/a
11	BATF	chr5:60034434-60034644	GM12878	blood:	n/a	n/a
12	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
13	BATF	chr5:60122447-60122875	GM12878	blood:	n/a	chr5:60122677-60122688
14	BATF	chr5:60122489-60122819	GM12878	blood:	n/a	chr5:60122677-60122688
15	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:60057304-60057451	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:60057285-60057534	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:60122417-60122906	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:60122515-60122796	GM12878	blood:	n/a	n/a
20	BCL3	chr5:60125467-60125724	GM12878	blood:	n/a	n/a
21	BCL3	chr5:60106438-60107052	A549	lung:	n/a	n/a
22	BCLAF1	chr5:60122249-60122828	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:60116487-60117300	K562	blood:	n/a	n/a
24	BHLHE40	chr5:60118549-60118717	K562	blood:	n/a	n/a
25	BHLHE40	chr5:60093321-60093343	K562	blood:	n/a	n/a
26	BHLHE40	chr5:60057135-60057471	HepG2	liver:	n/a	n/a
27	BHLHE40	chr5:60057704-60057885	HepG2	liver:	n/a	n/a
28	BHLHE40	chr5:60061785-60061831	K562	blood:	n/a	n/a
29	BRCA1	chr5:60077591-60077598	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr5:60116433-60116897	K562	blood:	n/a	n/a
31	CBX3	chr5:60036251-60036420	K562	blood:	n/a	n/a
32	CBX3	chr5:60116199-60117217	K562	blood:	n/a	n/a
33	CCNT2	chr5:60116540-60117162	K562	blood:	n/a	n/a
34	CCNT2	chr5:60087265-60087434	K562	blood:	n/a	n/a
35	CEBPB	chr5:60076330-60076558	A549	lung:	n/a	n/a
36	CEBPB	chr5:60050748-60051054	HepG2	liver:	n/a	chr5:60050867-60050878 chr5:60050867-60050880 chr5:60050869-60050878
37	CEBPB	chr5:60126458-60126748	A549	lung:	n/a	chr5:60126571-60126582
38	CEBPB	chr5:60100558-60100826	HepG2	liver:	n/a	chr5:60100694-60100705 chr5:60100693-60100706 chr5:60100693-60100704
39	CEBPB	chr5:60122893-60123201	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:60102783-60102827	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:60106304-60107068	A549	lung:	n/a	n/a
42	CEBPB	chr5:60061191-60061480	K562	blood:	n/a	chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061344 chr5:60061331-60061342 chr5:60061331-60061344 chr5:60061333-60061342
43	CEBPB	chr5:60106418-60106811	A549	lung:	n/a	n/a
44	CEBPB	chr5:60113126-60113422	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:60117607-60117705	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:60135974-60136156	A549	lung:	n/a	n/a
47	CEBPB	chr5:60100612-60100784	A549	lung:	n/a	chr5:60100694-60100705 chr5:60100693-60100706 chr5:60100693-60100704
48	CEBPB	chr5:60101181-60101630	HCT-116	colon:	n/a	n/a
49	CEBPB	chr5:60061183-60061502	HepG2	liver:	n/a	chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061344 chr5:60061331-60061342 chr5:60061331-60061344 chr5:60061333-60061342
50	CEBPB	chr5:60071781-60071807	HepG2	liver:	n/a	chr5:60071781-60071792

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60073995-60074045	HMEC	breast:	n/a
2	chr5:60039819-60039869	HRE	kidney:	n/a
3	chr5:60059120-60059170	ovcar-3	ovarian:	n/a
4	chr5:60039819-60039869	HUVEC	blood vessel:	n/a
5	chr5:60059120-60059170	HEK293	kidney:	embryo
6	chr5:60040736-60040786	MCF10A-Er-Src	breast:	n/a
7	chr5:60038293-60038343	IMR90	lung:	fetal
8	chr5:60040736-60040786	HUVEC	blood vessel:	n/a
9	chr5:60073995-60074045	IMR90	lung:	fetal
10	chr5:60039819-60039869	T-47D	breast:	n/a
11	chr5:60040736-60040786	HCT-116	colon:	n/a
12	chr5:60050299-60050349	AG09319	gingival:	n/a
13	chr5:60073995-60074045	AG10803	skin:	n/a
14	chr5:60039648-60039698	HRE	kidney:	n/a
15	chr5:60059120-60059170	ECC-1	luminal epithelium:	n/a
16	chr5:60039414-60039464	HRCEpiC	kidney:	n/a
17	chr5:60039414-60039464	SK-N-SH	brain:	n/a
18	chr5:60038293-60038343	Hela-S3	cervix:	n/a
19	chr5:60039729-60039779	NB4	blood:	n/a
20	chr5:60132712-60132762	GM12878	blood:	n/a
21	chr5:60039414-60039464	HEK293	kidney:	embryo
22	chr5:60073995-60074045	U87	brain:	n/a
23	chr5:60039648-60039698	NHDF-neo	bronchial:	n/a
24	chr5:60039414-60039464	SK-N-SH_RA	brain:	n/a
25	chr5:60039729-60039779	NH-A	brain:	n/a
26	chr5:60039648-60039698	HEEpiC	esophagus:	n/a
27	chr5:60040736-60040786	NT2-D1	testis:	n/a
28	chr5:60039729-60039779	AG04449	skin:	fetal
29	chr5:60132712-60132762	HRPEpiC	eye:	n/a
30	chr5:60040736-60040786	HepG2	liver:	n/a
31	chr5:60040736-60040786	SAEC	small airway:	n/a
32	chr5:60038293-60038343	AG04450	lung:	fetal
33	chr5:60038293-60038343	HCPEpiC	choroid plexus:	n/a
34	chr5:60059120-60059170	HCF	heart:	n/a
35	chr5:60039819-60039869	NHBE	bronchial:	n/a
36	chr5:60038293-60038343	BE2_C	brain:	n/a
37	chr5:60040736-60040786	PANC-1	pancreas:	n/a
38	chr5:60038293-60038343	AG10803	skin:	n/a
39	chr5:60039414-60039464	RPTEC	kidney:	n/a
40	chr5:60073995-60074045	HRCEpiC	kidney:	n/a
41	chr5:60039414-60039464	AG09319	gingival:	n/a
42	chr5:60073995-60074045	PFSK-1	brain:	n/a
43	chr5:60038293-60038343	GM06990	blood:	n/a
44	chr5:60038293-60038343	U87	brain:	n/a
45	chr5:60039414-60039464	PANC-1	pancreas:	n/a
46	chr5:60039414-60039464	Hepatocyte	liver:	n/a
47	chr5:60039648-60039698	AoSMC	blood vessel:	n/a
48	chr5:60073995-60074045	AG09319	gingival:	n/a
49	chr5:60039648-60039698	ovcar-3	ovarian:	n/a
50	chr5:60039819-60039869	PFSK-1	brain:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
2	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
3	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
4	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
5	chr5:60131900..60133961-chr5:60138518..60140783,2	MCF-7	breast:
6	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
7	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
8	chr5:60134031..60135823-chr5:60138767..60140768,2	MCF-7	breast:
9	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
10	chr5:60106755..60108594-chr5:60111112..60113028,2	MCF-7	breast:
11	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
12	chr5:60119778..60121322-chr5:60121327..60122978,2	K562	blood:
13	chr5:60082437..60084997-chr5:60089364..60092082,2	MCF-7	breast:
14	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
15	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
16	chr5:60054901..60056742-chr5:60065532..60068314,2	K562	blood:
17	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
18	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
19	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
20	chr5:60017651..60020271-chr5:60037416..60040413,2	MCF-7	breast:
21	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
22	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
23	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
24	chr5:60104199..60107112-chr5:60138183..60141170,2	MCF-7	breast:
25	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
26	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
27	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
28	chr5:60046195..60048141-chr5:60138648..60140514,2	MCF-7	breast:
29	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
30	chr5:59928143..59930570-chr5:60056842..60058406,2	MCF-7	breast:
31	chr5:60106755..60108594-chr5:60111112..60113028,2	MCF-7	breast:
32	chr5:59993402..59996272-chr5:60048809..60051606,2	MCF-7	breast:
33	chr5:60101058..60102798-chr5:60106672..60109127,2	K562	blood:
34	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
35	chr5:60111228..60113761-chr5:60138428..60140266,2	MCF-7	breast:
36	chr5:59994794..59996427-chr5:60100174..60102513,2	K562	blood:
37	chr5:60090547..60092252-chr5:60093927..60095567,2	K562	blood:
38	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
39	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
40	chr5:60119778..60121322-chr5:60121327..60122978,2	K562	blood:
41	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
42	chr5:60090547..60092252-chr5:60093927..60095567,2	K562	blood:
43	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
44	chr5:60037106..60038817-chr5:60040553..60043083,2	MCF-7	breast:
45	chr5:59994096..59995835-chr5:60107793..60109955,2	MCF-7	breast:
46	chr5:60054901..60056742-chr5:60065532..60068314,2	K562	blood:
47	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
48	chr5:60101058..60102798-chr5:60106672..60109127,2	K562	blood:

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ELOVL7	hsa-miR-21-5p	chr5:60049832-60049858
2	ELOVL7	hsa-miR-21-5p	chr5:60048157-60048175

Variant related genes	Relation type
KRT8P31	TF binding region
ELOVL7	TF binding region
KRT8P31	CpG island
ELOVL7	CpG island
ENSG00000250148	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000035499	chromatin interactions

Extended variants
information (count: 3419 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3419 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12655977	chr5:60034475-60034476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114690186	chr5:60034548-60034549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550651484	chr5:60034583-60034584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571167089	chr5:60034621-60034622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138377726	chr5:60034645-60034646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188269635	chr5:60034653-60034654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567048335	chr5:60034655-60034656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546162729	chr5:60034670-60034671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539416889	chr5:60034672-60034673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1117677	chr5:60034675-60034676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs568115630	chr5:60034701-60034702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs180790608	chr5:60034705-60034706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187276542	chr5:60034707-60034708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576369050	chr5:60034795-60034796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73106101	chr5:60034803-60034804	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs561682459	chr5:60034812-60034813	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs545759707	chr5:60034823-60034824	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs1117676	chr5:60034824-60034825	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs141082218	chr5:60034851-60034852	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs1117675	chr5:60034886-60034887	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs561847782	chr5:60034926-60034927	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs377764148	chr5:60034932-60034933	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs530902909	chr5:60034966-60034967	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs1117674	chr5:60035007-60035008	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs75705005	chr5:60035043-60035044	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs552126674	chr5:60035047-60035048	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs547337690	chr5:60035135-60035136	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs10471493	chr5:60035222-60035223	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs72755192	chr5:60035261-60035262	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370107444	chr5:60035341-60035342	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs568202698	chr5:60035377-60035378	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs536734248	chr5:60035378-60035379	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs6887434	chr5:60035420-60035421	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs192175049	chr5:60035422-60035423	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539386214	chr5:60035484-60035485	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552861106	chr5:60035589-60035590	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568700880	chr5:60035604-60035605	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs138523793	chr5:60035609-60035610	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs181732547	chr5:60035637-60035638	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs6887637	chr5:60035640-60035641	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs547701498	chr5:60035681-60035682	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs575725800	chr5:60035689-60035690	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs111437594	chr5:60035739-60035740	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs144115907	chr5:60035764-60035765	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs577971576	chr5:60035910-60035911	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs540592796	chr5:60035929-60035930	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs114012600	chr5:60035940-60035941	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs529603306	chr5:60035993-60035994	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs549633704	chr5:60036005-60036006	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs557744479	chr5:60036031-60036032	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60025600-60035400	Weak transcription	Fetal Intestine Large	intestine
2	chr5:60032800-60035600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:60033200-60039200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:60034800-60035800	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr5:60035400-60035600	Strong transcription	Fetal Intestine Large	intestine
6	chr5:60035400-60035600	ZNF genes & repeats	Lung	lung
7	chr5:60035400-60036400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:60035600-60036000	ZNF genes & repeats	Fetal Intestine Large	intestine
9	chr5:60035600-60036200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:60035600-60036600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:60036200-60044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:60037400-60047600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:60039200-60039400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:60039200-60039600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:60039200-60040200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:60039600-60039800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:60039600-60041000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:60040600-60040800	ZNF genes & repeats	Fetal Intestine Small	intestine
19	chr5:60040800-60066600	Weak transcription	Fetal Intestine Small	intestine
20	chr5:60041200-60044000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:60042200-60050000	Weak transcription	Fetal Intestine Large	intestine
22	chr5:60042200-60052000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr5:60042600-60043000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:60042600-60055800	Weak transcription	Brain Hippocampus Middle	brain
25	chr5:60044000-60045000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:60044000-60046200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:60044800-60045200	ZNF genes & repeats	Brain Angular Gyrus	brain
28	chr5:60044800-60046000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:60044800-60081600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr5:60044800-60098000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr5:60045000-60045200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:60045000-60056600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr5:60045200-60048800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr5:60045200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr5:60045200-60084400	Weak transcription	Brain Angular Gyrus	brain
36	chr5:60046000-60061000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr5:60046200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:60050000-60051000	Strong transcription	Fetal Intestine Large	intestine
39	chr5:60051000-60057000	Weak transcription	Fetal Intestine Large	intestine
40	chr5:60056600-60058000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr5:60057000-60057600	Strong transcription	Fetal Intestine Large	intestine
42	chr5:60057600-60061200	Weak transcription	Fetal Intestine Large	intestine
43	chr5:60057600-60092200	Weak transcription	Brain Anterior Caudate	brain
44	chr5:60057600-60093200	Weak transcription	Pancreas	Pancrea
45	chr5:60057800-60074800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr5:60058000-60066200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:60060600-60069600	Weak transcription	Esophagus	oesophagus
48	chr5:60061000-60061800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:60061000-60062000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:60061200-60061600	Enhancers	Fetal Intestine Large	intestine

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